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Prophylaxis and treatment of experimental lung metastases in mice after treatment with liposome-encapsulated 6-O-stearoyl-N-acetylmuramyl-L-alpha-aminobutyryl-D-isoglutamine.

Abstract
A new lipophilic muramyl dipeptide analog, 6-O-stearoyl-N-acetylmuramyl-L-alpha-aminobutyryl-D-isoglutamine, when incorporated in liposomes, was effective in both the prevention and eradication of experimental pulmonary metastases in mice. Multilamellar vesicles composed of synthetic phospholipids (phosphatidylglycerol and phosphatidylcholine) containing saturated myristoyl or unsaturated dioleoyl acyl chains were found to potentiate the antimetastatic activity of this glycopeptide. Prophylactic and therapeutic efficacy was observed against the three murine tumors tested: FSa, an immunogenic fibrosarcoma; NFSa, a nonimmunogenic fibrosarcoma; and B16 melanoma. Neither the administration of empty liposomes or free glycopeptide, nor their coadministration, had a significant antimetastatic effect. This approach is promising for the therapy of cancer metastases in humans, particularly in the prevention of metastatic seeding and in the treatment of micrometastases.
AuthorsG Lopez-Berestein, L Milas, N Hunter, K Mehta, E M Hersh, C G Kurahara, M Vandupas, D A Eppstein
JournalClinical & experimental metastasis (Clin Exp Metastasis) 1984 Apr-Jun Vol. 2 Issue 2 Pg. 127-37 ISSN: 0262-0898 [Print] Netherlands
PMID6543694 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Liposomes
  • Acetylmuramyl-Alanyl-Isoglutamine
  • 6-O-stearoyl-N-acetylmuramyl-alpha-aminobutyryl-isoglutamine
Topics
  • Acetylmuramyl-Alanyl-Isoglutamine (administration & dosage, analogs & derivatives, therapeutic use)
  • Animals
  • Cell Line
  • Fibrosarcoma (pathology)
  • Liposomes
  • Lung Neoplasms (prevention & control, secondary)
  • Melanoma (pathology)
  • Mice

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